The Renilla luciferase gene as a reference gene for normalization of gene expression in transiently transfected cells

Meesbah Jiwaji, Rónán Daly, Kshama Pansare, Pauline McLean, Jingli Yang, Walter Kolch, Andrew Pitt

Research output: Contribution to journalArticle

Abstract

Background: The importance of appropriate normalization controls in quantitative real-time polymerase chain reaction (qPCR) experiments has become more apparent as the number of biological studies using this methodology has increased. In developing a system to study gene expression from transiently transfected plasmids, it became clear that normalization using chromosomally encoded genes is not ideal, at it does not take into account the transfection efficiency and the significantly lower expression levels of the plasmids. We have developed and validated a normalization method for qPCR using a co-transfected plasmid.Results: The best chromosomal gene for normalization in the presence of the transcriptional activators used in this study, cadmium, dexamethasone, forskolin and phorbol-12-myristate 13-acetate was first identified. qPCR data was analyzed using geNorm, Normfinder and BestKeeper. Each software application was found to rank the normalization controls differently with no clear correlation. Including a co-transfected plasmid encoding the Renilla luciferase gene (Rluc) in this analysis showed that its calculated stability was not as good as the optimised chromosomal genes, most likely as a result of the lower expression levels and transfection variability. Finally, we validated these analyses by testing two chromosomal genes (B2M and ActB) and a co-transfected gene (Rluc) under biological conditions. When analyzing co-transfected plasmids, Rluc normalization gave the smallest errors compared to the chromosomal reference genes.Conclusions: Our data demonstrates that transfected Rluc is the most appropriate normalization reference gene for transient transfection qPCR analysis; it significantly reduces the standard deviation within biological experiments as it takes into account the transfection efficiencies and has easily controllable expression levels. This improves reproducibility, data validity and most importantly, enables accurate interpretation of qPCR data.
LanguageEnglish
Pages103
JournalBMC Molecular Biology
Volume11
DOIs
Publication statusPublished - 31 Dec 2010

Fingerprint

Renilla Luciferases
Gene Expression
Genes
Real-Time Polymerase Chain Reaction
Plasmids
Transfection
Colforsin
Cadmium
Dexamethasone

Bibliographical note

© 2010 Jiwaji et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Keywords

  • animals
  • chromosomes
  • gene expression
  • HEK293 cells
  • humans
  • renilla luciferases
  • polymerase chain reaction
  • reference standards
  • software
  • transfection

Cite this

Jiwaji, Meesbah ; Daly, Rónán ; Pansare, Kshama ; McLean, Pauline ; Yang, Jingli ; Kolch, Walter ; Pitt, Andrew. / The Renilla luciferase gene as a reference gene for normalization of gene expression in transiently transfected cells. In: BMC Molecular Biology. 2010 ; Vol. 11. pp. 103.
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The Renilla luciferase gene as a reference gene for normalization of gene expression in transiently transfected cells. / Jiwaji, Meesbah; Daly, Rónán; Pansare, Kshama; McLean, Pauline; Yang, Jingli; Kolch, Walter; Pitt, Andrew.

In: BMC Molecular Biology, Vol. 11, 31.12.2010, p. 103.

Research output: Contribution to journalArticle

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AU - Yang, Jingli

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